V-shaped handpiece for dermabrasion

ABSTRACT

A dermabrasion apparatus operating by a flow of air and reducing substances conveyed by a pneumatic system through a handpiece. The apparatus comprises a housing, a vacuum pump, and an external tray inside of which a mixing bottle and a collecting bottle are provided. The handpiece and the bottles are disposable sterilized components, and may be kept in a plastic bag for maintaining their sterility prior to use. The components may be subjected to gamma rays while in the plastic bag, in order to provide an additional level of sterilization.

RELATED APPLICATIONS

The present application is a continuation-in-part of U.S. Ser. No. 09/099,523 filed Jun. 18, 1998, now U.S. Pat. No. 6,306,147, which is a continuation in part of Ser. No. 09/088,873 filed Jun. 2, 1998, abandoned which itself is a continuation-in-part of U.S. Ser. No. 08/496,470, filed Jun. 29, 1995 now U.S. Pat. No. 5,810,842, and U.S. Ser. No. 08/797,909 filed Feb. 10, 1997, now U.S. Pat. No. 6,120,512 all of which are incorporated in their entirety herein by reference.

FIELD OF THE INVENTION

The present invention relates to the field of the cosmetic and microsurgical treatments. In particular, the present invention relates to a microdermabrasion apparatus and to the components making up the apparatus, operating by a pressurized flow of air and reducing substances, preferably corundum.

BACKGROUND OF THE INVENTION

Several technical solutions to produce a microdermabrasion apparatus are already known, all comprising vacuum means and/or pressurizing means which send a flow of air and reducing substances on a tissue portion to be treated and then remove from that portion the abraded particles. A drawback of such systems is that the sterility of the various components is not guaranteed, without the use of complicated and expensive processes.

Italian patent application FI94A000131, which corresponds to U.S. application Ser. No. 08/496,470 and is incorporated in its entirety herein by reference, describes a dermabrasion apparatus operating by a flow of reducing substances. The apparatus comprises a compressor, a vacuum pump, and three detachable one-piece components. The components include a mixing bottle, a collecting bottle for the abraded particles and a handpiece to touch the tissue to be treated. These components are preferably made of glass or plastic material and can be easily sterilized.

However, potential drawbacks of such an apparatus include the fact that the air pressurization is performed by a compressor placed inside the apparatus, making it necessary to sterilize the air because, during treatment, the compressor could be infected by bacteria which would be afterwards conveyed on the patient's skin by the pneumatic system. Furthermore, while the above-mentioned one-piece components are sterilized after the apparatus has been used, they do not guarantee proper sterility when the apparatus performs succeeding treatments on different patients. A further drawback is that contamination can occur when the mixing bottle is filled with new reducing substances or when the collecting bottle is cleaned of the abraded particles.

SUMMARY OF THE INVENTION

An object of the invention is to ensure the sterility of the apparatus components in all circumstances, for instance when sterilization methods, such as UV rays or an autoclave, are not available. A further object of the invention is to obtain easy replaceable, low cost apparatus components.

The present invention provides a microdermabrasion apparatus having disposable sterilized components which include easily interchangeable one-piece blocks. Such components include a filled mixing bottle containing the reducing substances (preferably corundum), a collecting bottle for the receiving the abraded tissue particles of a patient, and a handpiece for providing the reducing substances to the patient to cause skin tissue of the patient to abrade during the treatment of the patient. The handpiece, the mixing bottle and the collecting bottle are manufactured and sealed in a sterilized environment. According to an embodiment of the invention, the handpiece, the mixing bottle and the collecting bottle are made of plastic material, preferably polycarbonate, in order to reduce costs, and to make them particularly suitable for disposable use. After manufacturing, the components can be packed in sterilized packagings which include either a single component (e.g., one of the mixing bottle, the collecting bottle, and the handle) or a multi-component kit. In this way, contamination risks are reduced from the manufacturing through use of the components. In order to avoid contaminating the abraded tissue with particles of the handpiece material abraded in use, the portion of the handpiece most subjected to the abrasion effect is an abrasion-proof block made of a suitably hard material, for example glass or ceramic. According to a first embodiment of the invention, the source of pressurized air, or of another suitable gas, is constituted by at least one disposable bottle of sterilized pressurized air. In this way, sterility is guaranteed to the apparatus components exposed to contamination risks for each treatment. A further advantage is low cost of production for such components. In an alternate configuration, a compressor may be utilized instead of a pressurized air source to provide an air/reducing substances mixture to disposable, single-use components, but this configuration may introduce contaminants into the reducing substances/air mixture that is applied to the patient by way of the handle.

The above-mentioned objects and other advantages maybe achieved by a collecting bottle for use in dermabrasion. The collecting bottle includes a cylindrical housing having a top surface and a bottom surface. The collecting bottle also includes a suction tube disposed within the housing at a substantially central location within the housing. The collecting bottle further includes a supply tube disposed within the housing for providing an air/reducing substances/abraded tissue mixture into the housing. The supply tube has a top, bent portion that is disposed along an axis that is substantially tangential to an outer circumference of the housing.

The above-mentioned objects and other advantages may also be achieved by a dermabrasion treatment kit. The kit includes a handle for applying dermabrading materials to a patient. The kit further includes a mixing bottle for providing an air/reducing substances mixture to the handle. The kit also includes a collecting bottle for receiving the air/reducing substances mixture from the handle after the air/reducing substances mixture has been applied to the patient. The kit still further includes a tray for holding the mixing bottle and the collecting bottle in place. The mixing bottle and the collecting bottle are positioned on the tray in a same orientation.

The above-mentioned objects and other advantages may also be achieved by a dermabrasion apparatus. The apparatus includes a mono-block which comprises a mixing bottle and a handle, the mixing bottle providing an air/reducing substances mixture to the handle for application to a patient.

The above-mentioned objects and other advantages may also be achieved by device for applying an air/reducing substances mixture to a patient. The device includes a handle. The devices also includes supply tube connected to the handle for providing the air/reducing substances mixture to the handle. The device further includes a collection tube connected to the handle for receiving the air/reducing substances mixture from the handle, after the air/reducing substances mixture has been applied to a patient, and for outputting the air/reducing substances mixture to a collecting region. The device still further includes a holding element configured to hold the supply tube, the collection tube, and the handle in place.

The above-mentioned objects and other advantages may also be achieved by a handpiece for dermabrasion of a patient. The handpiece includes a supply side that provides an air/reducing substances mixture to a patients skin. The handpiece further includes an opening for making contact with the patient's skin. The handpiece also includes a collecting side for receiving the air/reducing substances mixture and any abraded tissue from the patient after the air/reducing substances mixture has contacted the patient's skin. The supply side is positioned at a different angle with respect to the opening than the collecting side.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other objects and advantages of the invention will become more fully apparent from the following detailed description when read in conjunction with the accompanying drawings with like reference numerals indicating corresponding parts throughout, and wherein:

FIG. 1 schematically shows the layout of the apparatus according to a first embodiment of invention;

FIG. 2 shows a side view of the apparatus according to the first embodiment of the invention;

FIG. 3 shows a front view of the apparatus of FIG. 2;

FIG. 4 shows a first configuration according to the invention of the mixing bottle filled with reducing substances;

FIG. 5 shows a first configuration of the collecting bottle according to the invention;

FIG. 6 shows a first configuration of the contacting handpiece according to the invention, FIG. 7 shows a top view of the handpiece of FIG. 6;

FIGS. 8a, 8 b show different views of the abrasion-proof block of the handpiece of FIG. 6;

FIG. 9a shows one of the filters (or labyrinths) of the mixing bottle of FIG. 4;

FIG. 9b shows the other of the filters (or labyrinths) of the mixing bottle of FIG. 4;

FIG. 10 shows the fitting of the mixing bottle onto the external tray according to the present invention;

FIG. 11 shows another configuration of the contacting handpiece according to the present invention;

FIG. 12 shows yet another configuration of the contacting handpiece according to the present invention;

FIG. 13 shows another configuration of the collecting bottle according to the present invention;

FIG. 14 shows a top view of the other configuration of the collecting bottle according to the present invention;

FIG. 15 shows a path of reducing substances/abraded tissue within the other configuration of the collecting bottle according to the present invention;

FIG. 16 shows a second embodiment of the present invention, in which a mixing bottle and handle are a single, one-piece mono-block construction;

FIG. 17 shows a side view of a holding element and various items attached to it, according to a third embodiment of the invention;

FIG. 18 shows the holding element by itself, according to the third embodiment of the invention;

FIG. 19 shows a handpiece that can be utilized in the third embodiment;

FIG. 20 shows a top view of the holding element;

FIG. 21 shows a front-on view of the holding element;

FIG. 22 shows a supply tube that can be fitted onto the holding element;

FIG. 23 shows a fourth embodiment in which a collecting bottle and mixing bottle are positioned in a same orientation; and

FIGS. 24a-24 c show different views the handpiece according to the third embodiment, in which the air/reducing substances mixture is provided to the patient at an angle of 45 degrees; and

FIGS. 25a-25 d show different views of another alternative configuration of the handpiece according to the third embodiment, in which the air/reducing substances mixture is provided to the patient at an angle of 90 degrees.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring to FIGS. 1 and 2, a microdermabrasion apparatus 10 according to a first embodiment of the invention comprises a housing 11, a vacuum pump 12, a mixing bottle 15 containing the reducing substances, for example corundum or aluminum oxide (sand-like substance), and a collecting bottle 17 to collect the reducing substances and the abraded tissue particles after use. As shown in FIG. 1, apparatus 10 is connected by a pneumatic system to a handpiece 16, which is intended to contact the tissue portion (e.g., skin of a patient) during treatment of a patient. The first embodiment also provides a valve 13 controlled by a switch 14, for example a treadle or a hand-operated switch, able to switch the air inlet from two different sources 13′, 13″. In a first example, the first source is a bottle of pressurized and sterilized air, and the second source is air at ambient pressure. In another possible configuration, the switching operates between two pressurized bottles feeding the sterilized air at different levels of pressure, so that a user can vary the abrasion efficiency of the apparatus according to the treatment requirements without interrupting the treatment. The same effect can be achieved by providing a single source with two outlet connections adjusted to output the air at different pressures. Downstream from the collecting bottle 17 and upstream from the vacuum pump 12, there is also provided a filter 18 to stop small particles flowing accidentally from the collecting bottle 17. The filter 18 is an optional component, depending upon the degree of sterility desired.

FIG. 2 and FIG. 3 illustrate a preferred construction of the housing 11, which includes a casing 35, preferably made of plexiglass, and a bar 19 supporting the vacuum pump 12, where lateral flanges 20, 21 are connected by a threaded tie rod 22. Housing 11 further includes a tray 23, preferably an external tray, fixed to the flange 20 and housing the mixing bottle 15 and the collecting bottle 17. The tray 23 is preferably made of metal or plastic. Flange 21 holds the filter 18 placed upstream from the vacuum pump 12. Referring to FIG. 4, the mixing bottle 15 is a substantially cylindrical one-piece block obtained, for example, by ultrasound welding along a horizontal junction line 9. In FIG. 4, the junction line 9 is shown near the top portion of the mixing bottle 15, to allow for simpler manufacturing of the pieces making up the mixing bottle 15. Of course, the junction line 9 can be placed at any other location of the mixing bottle 15, while remaining within the scope of the invention. Alternatively, the mixing bottle 15 may be made from a one-piece construction, without any welding of sections required.

Mixing bottle 15 is provided with connection pipes 24, 25 connected respectively with valve 13, and with the pneumatic duct leading to the handpiece 16 according to the scheme of FIG. 1. Pipe connection 25 extends into the mixing bottle 15 with a suction tube 26 having a hole 26′ (or aperture) near the bottom wall of mixing bottle 15, through which the reducing substances are introduced into the pneumatic system. Preferably, hole 26′ is located at a position between {fraction (1/10)} and {fraction (3/10)} of the total height of the mixing bottle. This position of the hole 26′ is high enough on the pipe connection 25 such that an air/corundum mixture that passes through the hole 26′ and thereby into the pipe connection 25 is of sufficient density so as not to cause blockage of the hole 26′. Also, the position of the hole 26′ is low enough on the pipe connection 25 such that air introduced into the mixing bottle 15 causes sufficient vibration or movement of the corundum inside the mixing bottle 15, so as to create a desired air/reducing substances (or ‘air/cordundum’) mixture.

Tube 26 and the inner end of the pipe connection 24 are provided with labyrinths 40, 41 schematically shown in FIGS. 9a, 9 b, respectively. Labyrinths 40, 41 present a T section with radial passages through which the air can pass whereas there is avoided the accidental backflow of the corundum through the pipe 24 connection and the possible introduction of the same into the tube 26, during the transporting operation. Preferably, labyrinths 40, 41 have eight passages (or holes) symmetrically spaced on the top portion of thereof. Other numbers of passages may be envisioned while remaining within the scope of the invention. Each passage preferably has a diameter of about 1 millimeter, so as to provide air bubbles of a size that causes sufficient vibration and movement of the corundum within the mixing bottle 15. The air bubbles output from each hole of labyrinth 41 move upwards as streamlets of air, and cause vibratory movement of the corundum. The T-shape of the labyrinth 41 is structured such that, during non-operational states (i.e., when the hole 34 is uncovered), the corundum in the mixing bottle 15 only moves part-way into the top-T portion of each T-shape passage, and does not move into the bottom-T portion of each passage. This is due primarily to the non-fluidity of the corundum, which tends to bunch up like sand and not flow readily unless provided with air under pressure. Thus, back-flow of the corundum into the connection tube 24 is effectively prevented.

According to the first embodiment of the invention, the mixing bottle 15 is filled with the corundum in an aseptic (sterilized) environment and thereafter is closed, preferably by ultrasound welding, and then sealed by suitable plug 24′, 25′. In the one-piece, non-welded configuration, the corundum is placed into the mixing bottle, and then the mixing bottle is sealed by plugs 24′, 25′. For example, each plug 24′, 25′ can have a bottom rubber layer which is pierced by the extremities of corresponding connecting junctions of the external tray 23 when the plugs 24′, 25′ are fitted into the external tray 23. Alternatively, each plug 24′, 25′ may comprise an aluminum foil or strip, which is punctured when the mixing bottle 15 is fitted into the external tray 23. In such a way, the mixing bottle 15 is connected with the valve 13 and with the downstream handpiece 16.

FIG. 10 shows the fitting of the mixing bottle 15 onto the external tray 23. In FIG. 10, the external tray 23 includes two connection pipes 50, 52, which are preferably made of a silicone-based material, or plastic. Pipes 50, 52 are flexible and preferably transparent in color. Disposed inside pipes 50, 52 are metal rings 54, 56, respectively. Disposed outside pipes 50, 52 are rubber seals 58,60 which are snugly fit around pipes 50, 52. Rubber seals 58, 60 provide a strong air-tight seal when connection pipes 24, 25 are fitted against pipes 50, 52, respectively. When mixing bottle 15 is fitted onto external tray 23, the connection pipes 24, 25 are moved downward towards the pipes 50, 52, so as to cause piercing of the plugs 24′, 25′ by metal pipes 54, 56. That way, an air-tight connection is provided.

Referring to FIG. 6, the handpiece 16 according to a first configuration comprises a substantially elliptical one-piece block having the upper portion in the shape of a hollow elliptical cap 44. Handpiece 16 is provided with an inlet connection 27 corresponding to an inner tube 7 through which the air and the reducing substances enter into the elliptical cap 44. After use, the reducing substances are removed from the elliptical cap 44 by a second tube 8 and a corresponding outlet connection 28. The handpiece elliptical cap 44 presents an opening 34, the rim of which defines the patient's tissue portion impinged upon by the reducing substances ejected from tube 7. In the preferred embodiment, the opening 34 is angled such that the air/reducing substances mixture is provided to the patient's tissue at an angle of approximately 45 degrees. That way, there is less of a chance that the air/reducing substances adheres or clings to the skin left on the patient during treatment. For example, if the air/reducing substances mixture was provided to the patient at an angle of 90 degrees (i.e. in a direction straight into the tissue of the patient), then some of the mixture may lodge into the skin (dermis) of the patient, and not cause the desired “brushing” against the skin of the patient that the 45 degree angle approach provides. This adherence of the mixture to the patient's skin is generally undesirable, and may result in infection to the patient if not removed antiseptically. However, for some purposes, applying the mixture at an angle of 90 degrees may be suitable, and the present invention may be utilized with handpieces that provide the mixture at such an angle.

According to the first configuration of the handle according to the invention the upper end of tube 7, which is the part subjected to the highest abrasion, is provided with an insert block 7′, shown in FIGS. 8a, 8 b. Block 7′ is a cylinder having an internal diameter smaller than a diameter of the tube 7 to achieve a smaller flow area and thus increase the flow rate of the reducing substances. Block 7′ is made of a hard material, preferably glass or ceramic. In a first embodiment, handpiece 16 has two half parts 46 symmetrical with respect to line A of FIG. 7 and manufactured, for example, by injection molding, together with the corresponding half parts of tubes 7, 8. Before assembling, block 7′ is inserted into the upper end portion of tube 7 and the spherical cap 44 is attached so that the opening 34 corresponds to the block 7′. That is, an air/corundum mixture output from mixing bottle 15 goes through inlet connection 27, through inner tube 7 and then through insert block 7′, and finally contacts a patient's skin (not shown) covering opening 34. The covering of the opening 34 creates a vacuum, so as to cause the air/corundum mixture to flow towards the patient's skin. The air/corundum mixture under pressure causes abrasion of the patient's skin, and a skin/corundum/air mixture is passed through tube 8, through outer connection 28, and is collected by collecting bottle 17. After attachment of the elliptical cap 44, the assembly is closed, for example by ultrasound welding along line A and line B between the elliptical cap 44 and the lower body 46 (see FIGS. 6 and 7). Alternatively, the elliptical cap 44 is welded to the lower body 46 by a single injection molding operation. In the alternative configuration, the handpiece 16 corresponds to a unitary piece or mono-block, such as the U-shaped mono-block shown in FIG. 6 of the drawings, or the one shown in FIGS. 7 and 8 of U.S. patent application Ser. No. 08/496,470.

In a second configuration of the handle, as shown in FIG. 11, the contacting handpiece 16′ is a mono-block (single, non-separable unit) which includes an insert block 7′ situated in a curved portion at the top of the handpiece 16′. By this configuration, the air output from the insert block 7′ is directed towards the opening 34′, with the air direction being shown by the dashed line 88. The opening 34′ is positioned at a substantially central position of the handpiece 16′. A longitudinal axis of the handpiece 16′ that bisects the handpiece 16′ is shown by dashed line 92. In the second configuration of the handpiece, the handpiece 16′ is manufactured as a single piece (except of course the insert block 7′), without the need for combining sections to thereby form the handpiece. In a third embodiment, the insert block 7′ may be omitted, and instead the handpiece 16″ may be formed such that the location where the insert block 7′ is located in the second configuration is made narrower than other portions of the handpiece 16″, as shown in FIG. 12.

Referring to FIG. 5, there is shown a first configuration of the collecting bottle 17, placed downstream of the handpiece 16 and upstream of the vacuum pump 12, according to the pneumatic system scheme of FIG. 1. In this first configuration, the collecting bottle 17 has a cylindrical hollow one-piece block provided with two upper connections 29, 30, the first operating as inlet for the reducing substances from handpiece 16, the second as a passage for the air aspirated by vacuum pump 12. Connection 30 is provided with an air filter 30′ in order to avoid the passage of used reducing substances and of tissue abraded particles towards the vacuum pump 12.

Collecting bottle 17 is preferably assembled by welding (preferably ultrasound welding) along line 6, the upper portion including connections 29, 30. The welding is preferably to connect a small portion of the collecting bottle 17 to the rest of the collecting bottle 17. That way, it is easier to manufacture the two pieces making up the collecting bottle 17. Downstream from the collecting bottle 17 is disposed a filter 18 for filtering small particles passed through the filter 30′ and conveyed towards vacuum pump 12. Filter 18 is preferably disposed immediately downstream from collecting bottle 17. Advantageously, the connections of collecting bottle 17 and handpiece 16 are provided with plugs, similar to previously described plugs 24′, 25′ which are intended to seal both collecting bottle 17 and handpiece 16 until their initial use, and to allow a quick and easy connection to the pneumatic system. In a second configuration, the collecting bottle may be made from a single-piece (mono-block) construction, without the need for welding of sections.

FIG. 13 shows a collecting bottle 17′ according to a second configuration, which may be constructed as either a mono-block or by welding of sections (as in the first configuration). In FIG. 13, the collecting bottle 17′ is configured such that it is placed onto the tray 23 with the plug-side down (e.g., in the orientation as shown in the figure). To accommodate such a placement of the collecting bottle 17′, the tube 1320 that provides the air/reducing substances/abraded tissue mixture to the inside of the collecting bottle 17′ is made almost as long as the length of the collecting bottle 17′. The tube 1320 is preferably at least 80% the length of the collecting bottle 17′.

In the second configuration, the collecting bottle preferably has a radius of about 2.5 cm, and a length of about 7 cm, but of course other sizes are possible. The tube 1320 ends at a position within a few millimeters of the top surface 1340 of the collecting bottle 17′. Also, the tube 1300 (also called “suction tube” hereinbelow) that provides the suction from the vacuum pump 12 to the collecting bottle 17′ (and thereby to the handle) is made almost as long as the length of the collecting bottle 17′. Again, the length of the tube 1300 is preferably at least 80% of the collecting bottle 17′. Furthermore, the suction tube 1300 is positioned such that its topmost, receiving end is located at a central position within the cylindrically-shaped collecting bottle 17′. This can be done by either positioning the connection 30 such that it is located at a central position on the bottom of the collecting bottle 17′ and then providing a tube 1300 that is straight. Alternatively, this can be done by positioning the connection 30 at another, non-central location, and then utilizing a non-straight tube 1300 that has its end portion located at a substantially central location near the top of the collecting tube 17′.

Referring now to FIG. 14, the tube 1310 has a 90 degree bent portion 1320 at the top of the tube 1310, where that bent portion 1320 is positioned about 2 mm away from the outer periphery of the collecting bottle 17. With this configuration, the air/reducing substances/abraded tissue mixture exits the bent portion 1310 of the tube 1320 and moves in a direction tangential (or substantially tangential) to a circumference of the cylindrical collecting bottle 17′. In other words, the bent portion 1320 is positioned such that it is substantially perpendicular to an imaginary line 1370 that is drawn to the center of the cylindrical collecting bottle 17′. With this second configuration, the air/reducing substances/abraded tissue mixture comes out of the bent portion 1320 of the tube 1310 in such a manner that the reducing substances/abraded tissue portion of that mixture follows the periphery of the collecting bottle 17′, to thereby create a vortex, and thereby makes its way down to the bottom of the collecting bottle 17′. The kinetic energy of the air/reducing substances/abraded tissue mixture, as it comes out of the bent portion 1320, is such that the kinetic energy is converted to a centrifugal force that makes the reducing substances/abraded tissue portion of the air/reducing substances/abraded tissue mixture follow a path close to the periphery of the cylindrical collecting bottle 17′ all the way down to the bottom portion of the collecting bottle 17′, where that mixture comes to rest. As such, the reducing substances/abraded tissue portion of the mixture does not come into contact with the middle portion of the collecting bottle 17′ as it makes its way down to the bottom of the collecting bottle 17′. This lessens the possibility that the filter 30′ will become clogged due to the reducing substances/abraded tissue adhering to it. Also, this lessens the possibility of the reducing substances/abraded tissue entering the vacuum hole at the top portion of the tube suction 1300.

The kinetic energy is not strong enough to maintain the air along the outer periphery path 1410 (see FIG. 15), but rather the air, being of course lighter than either the reducing substances or the abraded tissue, is sucked into a central location of the collecting bottle 17′ where the suction tube 1300 is positioned, and thereby makes its way through the suction tube 1300 and towards the vacuum pump 12. With such an approach, and with the filter 30′ preferably located at a position such that it will not come into contact with the reducing substances/abraded tissue mixture (e.g., positioned a few centimeters above the bottom portion of the collecting bottle 17′, clogging to the filter 30′ will not occur.

In an alternative configuration of the collecting bottle 17′, the filter 30′ may not be provided at all, since the reducing substances/abraded tissue mixture will not be directed to the vacuum tube 1300 by way of the configuration of the vacuum tube 1300 and the tube 1310 (and its bent portion 1320). FIG. 15 shows a path 1410 of the air/reducing substances/abraded tissue mixture as it leaves the bent portion 1320 of the tube 1310 and makes its way down, as a vortex following the shell of the collecting bottle 17′, down to the bottom portion of the collecting bottle 17′, where it comes to rest as reducing substances/abraded tissue mixture 1420. The vortex separates the air of the air/reducing substances/abraded tissue mixture from the reducing substances/abraded tissue portion, as the reducing substances/abraded tissue portion follows the periphery of the collecting bottle (see line 1410 of FIG. 15) as the air is sucked into the central portion where the suction tube 1300 is located (see FIG. 13 and FIG. 14).

After manufacture, the mixing bottle, the collecting bottle and the handpiece can be packaged, individually or in a kit including either all three components or at least the handpiece and collecting bottle, in sterilized packaging. The connection tubes can optionally be included in the kit. By having a disposable mixing bottle 15 that is manufactured and sent with seals 24′, 25′ to a user or operator, the user does not have to worry about bacteria or the like entering the mixing bottle 15, since it has already been sterilized (by gamma rays, for example) during manufacturing. Also, each mixing bottle may also have a silica-gel package or other type of desiccant disposed within the mixing bottle along with the corundum. The silica-gel package keeps any moisture from forming inside the mixing bottle, thereby keeping the corundum from clumping up and causing problems in the system. That way, a heating element to keep the corundum dry inside the mixing bottle is not required in the present invention.

The one-piece blocks according to the invention constitute a kit of disposable components which does not require the steps of: filling the mixing bottle with the reducing substances, cleaning the abraded particles from the collecting bottle and handpiece, or sterilizing critical parts of the apparatus. These steps were required in conventional devices, and represented additional time and money spent to achieve treatment safety. In the present invention, it is also possible to set an expiration time for the sterility condition of the blocks individually or as contained in the unique kit packaging. Upon reaching the expiration time, all critical parts of the apparatus can be safely and quickly replaced due in part to the described sealing plugs 24, 25, used to connect handpiece 16, 16′, or 16″ with the mixing bottle 15 and the collecting bottle 17 or 17′. Preferably, the blocks are ‘single-use’ blocks that are to be disposed after a single treatment of a patient.

The blocks can be made of any suitable plastic or vitreous material. A polycarbonate is preferred because it is a low cost material and can be sterilized by an autoclave when reuse of one or more components is needed. Alternatively, a polystrene structure or the like may be used. According to a further feature of the invention, the kit components can be manufactured in different colors in order to allow a better identification of their functions by the user, or can be transparent to allow the user to visually detect any contamination particles remaining after sterilization.

Furthermore, due to the disposable nature of the present invention, the mixing bottle and the handle can be manufactured as a single unit, or mono-block, without any way of removing or separating these components from each other. Since each component is to be thrown away after treatment of a patient, having a mono-block structure of a handle and mixing bottle is not a problem, since these components are not to be cleaned after treatment, but rather discarded. Such a configuration would not require a flexible tubing between the mixing bottle and the handle, but rather the entire one-piece construction can be made of ceramic or glass or the like.

FIG. 16 shows a second embodiment of the present invention, which is a mono-block comprising a mixing bottle and a handle. The entire structure shown in FIG. 16 is a one-piece construction, and where the mixing bottle portion 15′ and the handle portion 16′″ together comprise the mono-block structure. In another possible configuration, the mixing bottle, the collecting bottle and the handle all together can be manufactured as a single, mono-block structure, to be disposed after treatment of a patient. As mentioned above, since there is no need to clean each component after treatment of a patient, as is required by conventional dermabrasion apparatuses, having a mono-block structure which combines more than one element (such as a mixing bottle and a handle; or a handle and a collecting bottle; or a handle, mixing bottle, and collecting bottle), the entire mono-block structure is disposed after treatment, and thus there is no need to connect individual components together as is required for conventional dermabrasion apparatuses.

FIG. 17 shows a side view of a holding element 1710 for a handpiece 1720, according to a third embodiment of the present invention. FIG. 18 shows a side view of the holding element 1710 by itself, and FIG. 19 shows a side view of the handpiece 1720 that is sized to be fitted onto the holding element, along with a collecting tube 1740 and a supply tube 1750. FIG. 20 shows a top view of the holding element 1710. Referring now to FIGS. 17 and 18, the handpiece 1720 is fitted onto one side of the holding element 1710, and the collecting portion 1740 and supply portion 1750 are also fitted onto the respective legs of the handpiece 1720. The groove 1770 on the top of the holding element 1710 is sized to snugly hold the collecting portion 1740 in place, by slight application of pressure (e.g., by hand typically) to fit the collecting tube within the groove 1770. FIG. 21 shows a front-on view of the holding element 1710 showing the groove 1770 and the groove 1780. The grooves 1770, 1780 are each constructed with an opening having an angle greater than 180 degrees, for example, 190 degrees, with an opening that is sized to the diameter of the respective tubes 1740, 1750. By this configuration, the collecting portion 1740 can be fitted into the groove 1770 by easy manipulation of the collecting portion 1740 into the holding element 1710. A similar approach is performed for the supply portion 1750, which is fitted into the groove 1780 on the opposite side of the holding element 1710. The grooves 1770, 1780 are preferably about 0.5 cm deep, and of course are sized to the size of the tubes 1740, 1750 that are to be fitted into the grooves.

The holding element 1710 has deeper groove sections 1785, 1790 for holding the end portion of the supply and collecting portions 1740, 1750 in place. The depth of the groove sections 1785, 1790 are preferably about 0.8 cm deep, and of course are sized to the end sizes of the tubes 1740, 1750. FIG. 22 shows the supply portion or supply path 1750, which includes a larger-sized end portion 1755, and it is that end portion 1755 that is fitted into the groove section 1790, with a similar configuration for the collection tube 1740. The groove section 1790 is sized to have the larger-sized end portion 1755 snugly fit therein when pushed into the groove section 1790. The groove section 1785 is also sized to have the larger-sized end portion (not shown) of collection portion or collection path 1740 fit therein when pushed into the groove section 1785. The larger-sized end portions of the collection portion 1740 and the supply portion 1750 are sized to fit into the respective legs of the handpiece 1720.

By this configuration, the handpiece 1720 is held in place at one end of the holding element 1710, so that an operator can hold the holding piece in order to apply the small-sized handpiece 1720 to various locations on a patient's skin. Since the handpiece 1720 itself is fairly small, about 2.5 cm length from the top portion to the ends of each leg, holding the handpiece by itself without the aid of the holding element is relatively difficult. The holding element 1710, which is about 10 cm wide and about 5 cm high at its middle section, allows the operator to make precise treatments to the patient's skin by holding on to the holding element 1710 when treating the patient. As shown in FIG. 17, the holding element 1710 tapers to about a 2 cm height at its respective left and right sides, and has a maximum height at its middle portion.

Referring now to FIG. 20, the holding element 1710 is preferably constructed from two separate pieces, held in place by screws 2010, 2020 and washers 2030, 2040. The dot-dash-dot line in FIG. 20 shows where the two pieces making up the holding element 1710 meet. The holding element 1710 is preferably constructed from plexiglass, plastic or other lightweight material, to allow for ease of use. Alternatively, the holding element 1710 may be a single, unitary block that does not require screws to hold individual portions in place.

FIG. 23 shows a fourth embodiment of the invention, in which a mixing bottle 2115 and a collecting bottle 2117 are provided as a single, unitary component, to allow for ease in inserting the mixing bottle 2115 and the collecting bottle 2117 into a tray, such as tray 23 as shown in FIG. 2. In the first embodiment of FIG. 2, the collecting bottle 17 and the mixing bottle 15 are configured to be fitted into the tray in the orientations as shown in FIGS. 4 and 5. That is, the mixing bottle 15 is to be fitted into the tray 23 with its connections 24, 25 positioned at the bottom, while the collecting bottle 17 is to be fitted into the tray 23 with its connections 29, 30 positioned at the top. However, by utilizing the structure of the collecting bottle 17′ of FIG. 13, the collecting bottle 17′ can also be fitted into the tray 23 in a manner like the mixing bottle, that being with its connections positioned at the bottom (in the orientation as shown in FIG. 13). As such, the mixing bottle and the collecting bottle can be fitted into the tray at the same time using the single, unitary component structure of FIG. 23. Alternatively, the collecting bottle and the mixing bottle may be separate components, but may then be affixed to each other, such by use of a rubber band or the like, and then fitted onto the tray.

FIGS. 24a-24 c show different views of the handpiece 1720 that can be fitted into the holding element 1710, or which can be utilized without the holding element 1710 in order to dermabrade the skin of a patient. FIG. 19 shows a side view of the handpiece 1710, in which the air/reducing substances mixture is applied at an angle of 45 degrees, and where a venturi 1950 (made of glass or ceramic, preferably) is positioned in the supply path 1910. The collection path 1920 is positioned at a 90 degree angle with respect to the opening 1930 that directs the air/reducing substances mixture onto a patient's skin. The collection path 1920 receives an air/reducing substances/abraded tissue mixture, where the abraded tissue corresponds to tissue from the patient's skin. The collection path 1920 receives the air/reducing substances/abraded tissue mixture by way of a suction provided on the collection path 1920. FIG. 24a shows a view along a plane in which the supply path 1910 and the collection path 1920 are both disposed. A head portion of the handpiece has a slightly greater diameter than a remaining portion of the handpiece, with the head portion being integrally formed with the remaining portion. FIG. 24b shows a view of the handpiece 1720 looking directing into the opening 1930. FIG. 24d shows the handpiece looking directly into the supply path 1910.

FIGS. 25a-25 d show an alternative configuration of the handpiece of the third embodiment. In this alternative configuration, as seen best in the side view of FIG. 25a, a handpiece 2410 has a supply path 2420 (with a venturi 1950 fitted therein) that is positioned at a 45 degree angle with respect to the opening 2430, so as to provide the air/reducing substances mixture at an angle of 90 degrees with respect to the patient's skin. The handpiece 1720 of FIG. 19 and FIGS. 24a-24 c has a collection path 1920 that receives the air/reducing substances/abraded tissue mixture at an angle of 90 degrees with respect to the patient's skin. In the alternate configuration of FIGS. 25a-25 d, the handpiece 2410 has a collection path 2430 that receives the air/reducing substances/abraded tissue mixture at an angle of 45 degrees. FIG. 25b shows a view along a plane in which both the supply path 2420 and the collection path 2430 of the handpiece 2410 are disposed. A head portion of the handpiece 2410 has a slightly greater diameter than a remaining portion of the handpiece 2410, with the head portion being integrally formed with the remaining portion. FIG. 25c shows a view of the handpiece 2410 looking directing into the opening 2440. FIG. 24c shows the handpiece 2410 looking directly into the supply path 2420.

Further alternate configurations of the handpiece of the third embodiment can be contemplated while remaining within the scope of the invention, in which the collection path receives the air/reducing substances/abraded tissue mixture at an angle between 45 degrees and 90 degrees. While various configurations of a handpiece have been described with respect to the third embodiment, these handpieces may be utilized without a holding element, if desired.

The second, third and fourth embodiments may be utilized with a pressurized system, or with a compressor system, or with an aspirated system.

While preferred embodiments have been described herein, modification of the described embodiments may become apparent to those of ordinary skill in the art, following the teachings of the invention, without departing from the spirit and scope of the invention as set forth in the appended claims.

For example, after manufacturing of the disposable components making up the dermabrasion kit, such as the mixing bottle, the collecting bottle, the handle, and the pipes or tubes (preferably bendable plastic) that connect these elements together, they can then be placed in a bag, and then sealed. The components may be totally sterilized prior to placement in the bag. Alternatively, the components may be not sterilized or may only be partially sterilized prior to placement in the bag. The bag is preferably a sealable plastic bag (e.g., polyethelene). After the components have been placed in the bag, the bag is then subjected to gamma rays, in order to sterilize the components in the bag. That way, for the first case where the components are sterilized prior to placement in the bag, any contaminants introduced into the components during the placement of the components into the bag (and due to any impurities in the bag itself) would be removed, and, for the second case where the components were not sterilized or were only partially sterilized prior to placement in the bag, the complete sterilization of the components is performed while the components are in the sealed bag by the application of gamma rays to the bag. The second case allows for manufacturing of the components in a non-sterile or partially-sterile environment, which would typically save on costs involved in the manufacturing of the collecting bottle, the mixing bottle, and the handle. The use of gamma rays applied to components in a sealed bag also applies to the embodiment where several components are integrally connected to each other, such as the integral mixing bottle/handle structure shown in FIG. 16 together with a collecting bottle, or a single integral structure of a mixing bottle, a handle and a collecting bottle that does not require any pipes to connect these elements together (since they are already integrally formed as a single unit or monoblock).

Also, while the present invention has been described using a mixing bottle and a collecting bottle, other shapes besides a ‘bottle shape’ for mixing and collecting of an air/reducing substances mixture may be contemplated while remaining within the scope of the invention as described herein. For example, the components may be of rectangular shape or of a more complex (e.g., tetrahedron) shape. 

What is claimed is:
 1. A V-shaped handpiece, comprising: a supply side that provides an air/reducing substances mixture to a patient's skin, the supply side being a first linear extension of the handpiece that corresponds to a first leg of the V-shaped handpiece; an opening for making contact with the patient's skin; and a collecting side for receiving the air/reducing substances mixture and any abraded tissue from the patient after the air/reducing substances mixture has contacted the patient's skin, the collecting side being a second linear extension of the handpiece that corresponds to a second leg of the V-shaped handpiece, wherein the supply side is positioned at a different angle with respect to the opening than the collecting side, wherein the first linear extension is in direct alignment with respect to a plane in which the opening is located, wherein the second linear extension is not in direct alignment but instead is offset with respect to the plane of the opening, wherein the opening, when viewed along a path corresponding to the first imaginary line, is larger in size than a through path corresponding to the supply side, and wherein the opening, when viewed along a path corresponding to the second imaginary line, is equal in size to a through path corresponding to the collecting side.
 2. A V-shaped handpiece, comprising: a supply side that provides an air/reducing substances mixture to a patient's skin, the supply side being a first linear extension of the handpiece that corresponds to a first leg of the V-shaped handpiece; an opening for making contact with the patient's skin; and a collecting side for receiving the air/reducing substances mixture and any abraded tissue from the patient after the air/reducing substances mixture has contacted the patient's skin, the collecting side being a second linear extension of the handpiece that corresponds to a second leg of the V-shaped handpiece, wherein the supply side is positioned at a different angle with respect to the opening than the collecting side, wherein the second linear extension is in direct alignment with a plane in which the opening is located, wherein the first linear extension is not in direct alignment but instead is offset with respect to the plane of the opening, wherein the opening, when viewed along a path corresponding to the second imaginary line, is equal in size to a through path corresponding to the supply side, and wherein the opening, when viewed along a path corresponding to the first imaginary line, is larger in size than a through path corresponding to the collecting side.
 3. A V-shaped handpiece, comprising: a supply side that provides an air/reducing substances mixture to a patient's skin, the supply side being a first linear extension of the handpiece that corresponds to a first leg of the V-shaped handpiece; an opening for making contact with the patient's skin; a collecting side for receiving the air/reducing substances mixture and any abraded tissue from the patient after the air/reducing substances mixture has contacted the patient's skin, the collecting side being a second linear extension of the handpiece that corresponds to a second leg of the V-shaped handpiece; and a venturi positioned in the supply side, wherein the supply side is positioned at a different angle with respect to the opening than the collecting side, and wherein the venturi is positioned only in the supply side and no venturi is provided in the collecting side.
 4. A V-shaped handpiece, comprising: a supply side that provides an air/reducing substances mixture to a patient's skin, the supply side being a first linear extension of the handpiece that corresponds to a first leg of the V-shaped handpiece; an opening for making contact with the patient's skin; and a collecting side for receiving the air/reducing substances mixture and any abraded tissue from the patient after the air/reducing substances mixture has contacted the patient's skin, the collecting side being a second linear extension of the handpiece that corresponds to a second leg of the V-shaped handpiece, wherein the supply side is positioned at a different angle with respect to the opening than the collecting side, wherein the handpiece is about 2.5 cm in length from the opening to a far end of the supply side furthest from the opening, and wherein the handpiece is about 2.5 cm in length from the opening to a far end of the collecting side further from the opening. 